| NDC Code | 0093-7485-12 |
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| Package Description | 2 BLISTER PACK in 1 BOX (0093-7485-12) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-7485-19) |
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| Product NDC | 0093-7485 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Granisetron Hydrochloride |
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| Non-Proprietary Name | Granisetron Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20080102 |
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| End Marketing Date | 20190930 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078080 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | GRANISETRON HYDROCHLORIDE |
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| Strength | 1 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
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